Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Class Implantable

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Modulus ALIF Trial Rasp, 12x34x24 25°
Nuvasive, Inc.
1300116
In Commercial Distribution

  • 00195377050502 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial Rasp, 10x34x24mm 2
Nuvasive, Inc.
1300115
In Commercial Distribution

  • 00195377050496 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial Rasp, 8x34x24mm 25
Nuvasive, Inc.
1300114
In Commercial Distribution

  • 00195377050489 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial Rasp, 6x34x24mm 25
Nuvasive, Inc.
1300113
In Commercial Distribution

  • 00195377050472 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 12x34x24mm 20°
Nuvasive, Inc.
1300112
In Commercial Distribution

  • 00195377050465 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 10x34x24mm 20°
Nuvasive, Inc.
1300111
In Commercial Distribution

  • 00195377050458 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 8x34x24mm 20° S
Nuvasive, Inc.
1300110
In Commercial Distribution

  • 00195377050441 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 6x34x24mm 20° S
Nuvasive, Inc.
1300109
In Commercial Distribution

  • 00195377050434 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 12x34x24mm 15°
Nuvasive, Inc.
1300108
In Commercial Distribution

  • 00195377050427 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial Rasp, 10x34x24mm 15°
Nuvasive, Inc.
1300107
In Commercial Distribution

  • 00195377050410 ()


  • Internal spinal fixation procedure kit, reusable
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